Business · 06/04/2012Updated: 10/17/2026 · 1 min read
FDA Publishes Guidance for Industry and Food and Drug Administration Staff on Section 513(g) Requests for Information
Summary
The Food and Drug Administration (FDA) has released a new guidance document outlining procedures for submitting, reviewing, and responding to requests for information about medical device classifications under the Federal Food, Drug, and Cosmetic Act.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →